Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
- NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
- NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_assertion evidence source_evidence_literature NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
- NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_assertion SIO_000772 10581037 NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
- NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_assertion wasDerivedFrom befree-20150227 NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
- NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_assertion wasGeneratedBy ECO_0000203 NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.